Canonical Allele Identifier: PA2580305081
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1794703
ClinVar RCV Id: RCV002437332 RCV003102109
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Thr37Ile
CA382769764
NM_004588.5:c.110C>T